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(S)-N-benzyl-O-(3-ethoxycarbonylacryloyl)mandelamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 503185-09-9 Structure
  • Basic information

    1. Product Name: (S)-N-benzyl-O-(3-ethoxycarbonylacryloyl)mandelamide
    2. Synonyms:
    3. CAS NO:503185-09-9
    4. Molecular Formula:
    5. Molecular Weight: 367.401
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 503185-09-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (S)-N-benzyl-O-(3-ethoxycarbonylacryloyl)mandelamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-N-benzyl-O-(3-ethoxycarbonylacryloyl)mandelamide(503185-09-9)
    11. EPA Substance Registry System: (S)-N-benzyl-O-(3-ethoxycarbonylacryloyl)mandelamide(503185-09-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 503185-09-9(Hazardous Substances Data)

503185-09-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 503185-09-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,3,1,8 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 503185-09:
(8*5)+(7*0)+(6*3)+(5*1)+(4*8)+(3*5)+(2*0)+(1*9)=119
119 % 10 = 9
So 503185-09-9 is a valid CAS Registry Number.

503185-09-9Downstream Products

503185-09-9Relevant articles and documents

Stereoselective formation of optically active 2-oxy-1,3-oxazolidin-4-ones from chiral O-acylmandelamides or lactamides

Kamimura, Akio,Omata, Yoji,Kakehi, Akikazu,Shirai, Masashi

, p. 8763 - 8770 (2007/10/03)

(-)-O-Acyllactamides or mandelamides in the presence of TBSOTf underwent cyclization reaction to give optically active 2-oxy-1,3-oxazolidin-4-ones, a novel nitrogen analog of orthoesters, in good yields. An X-ray analysis and NOE studies indicated that the absolute configuration at the newly formed chiral carbon was S. For their synthetic application, the 1,3-dipolar cycloaddition of nitrile oxide was examined. The cycloadducts were obtained in a stereoselective manner. Subsequent treatment of the adduct with TBAF resulted in the one-step removal of mandelamide, giving optically active 4,5-dihydroisoxazole and mandelamide in good yields.

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